# K010175: Microlight 830 Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Microlight Corporation of America
- Decided: Feb 6, 2002 after 384 days
- Product code: NHN (Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
88 later devices descend from it; 11 cite it directly.
0 of 89 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K030692: Power Laser 90 (2003), 65 descendants of its own
- K070516: Powerlaser (2007), 63 descendants of its own
- K083595: Ezlase (2009), 58 descendants of its own
- K121286: EPIC 10 (2012), 31 descendants of its own
- K123971: Cynosure 1064NM Diode Laser (2013), 25 descendants of its own

Source page: https://510kreport.com/device/K010175
Methodology: https://510kreport.com/methodology